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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935071copy number variation1nstd209human GRCh38 chr17: 42,014,418-42,015,231 , GRCh37.p13 chr17: 40,166,436-40,167,249 , GRCh37.p13 chr17|NW_003571052.1: 301,060-301,873 DNAJC7
    nsv5930440copy number variation1nstd209human GRCh38 chr17: 42,003,950-42,007,837 , GRCh37.p13 chr17: 40,155,968-40,159,855 , GRCh37.p13 chr17|NW_003571052.1: 290,592-294,479 DNAJC7
    nsv5884798copy number variation1nstd209human GRCh38 chr17: 42,004,008-42,007,537 , GRCh37.p13 chr17|NW_003571052.1: 290,650-294,179 , GRCh37.p13 chr17: 40,156,026-40,159,555 DNAJC7
    nsv5562780sequence alteration1nstd206human GRCh38 chr17: 41,964,018-42,255,340 , GRCh37.p13 chr17|NW_003571052.1: 250,660-412,535 , GRCh37.p13 chr17: 40,116,036-40,277,911 KAT2A, STAT5B, 13 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5529921copy number variation1nstd206human GRCh38 chr17: 42,014,393-42,015,232 , GRCh37.p13 chr17|NW_003571052.1: 301,035-301,874 , GRCh37.p13 chr17: 40,166,411-40,167,250 DNAJC7
    nsv5520090copy number variation1nstd206human GRCh38 chr17: 42,007,949-42,008,554 , GRCh37.p13 chr17|NW_003571052.1: 294,591-295,196 , GRCh37.p13 chr17: 40,159,967-40,160,572 DNAJC7
    nsv5515998copy number variation1nstd206human GRCh38 chr17: 42,014,642-42,015,021 , GRCh37.p13 chr17|NW_003571052.1: 301,284-301,663 , GRCh37.p13 chr17: 40,166,660-40,167,039 DNAJC7
    nsv5325648copy number variation1nstd204human GRCh38.p13 chr17: 41,981,332-41,981,602 , GRCh37.p13 chr17: 40,133,350-40,133,620 , GRCh37.p13 chr17|NW_003571052.1: 267,974-268,244 DNAJC7
    nsv5321435copy number variation1nstd204human GRCh38.p13 chr17: 42,014,432-42,015,207 , GRCh37.p13 chr17|NW_003571052.1: 301,074-301,849 , GRCh37.p13 chr17: 40,166,450-40,167,225 DNAJC7
    nsv5150360mobile element insertion1nstd203human GRCh38 chr17: 42,009,986-42,010,002 , GRCh37.p13 chr17: 40,162,004-40,162,020 , GRCh37.p13 chr17|NW_003571052.1: 296,628-296,644 DNAJC7
    nsv5148044mobile element insertion1nstd203human GRCh38 chr17: 41,999,614-41,999,664 , GRCh37.p13 chr17|NW_003571052.1: 286,256-286,306 , GRCh37.p13 chr17: 40,151,632-40,151,682 DNAJC7
    nsv5016408copy number variation1nstd200human GRCh38 chr17: 42,008,272-42,010,398 , GRCh37.p13 chr17|NW_003571052.1: 294,914-297,040 , GRCh37.p13 chr17: 40,160,290-40,162,416 DNAJC7
    nsv5016407copy number variation1nstd200human GRCh38 chr17: 41,999,402-41,999,650 , GRCh37.p13 chr17: 40,151,420-40,151,668 , GRCh37.p13 chr17|NW_003571052.1: 286,044-286,292 DNAJC7
    nsv5016406copy number variation1nstd200human GRCh38 chr17: 41,980,469-41,981,107 , GRCh37.p13 chr17: 40,132,487-40,133,125 , GRCh37.p13 chr17|NW_003571052.1: 267,111-267,749 DNAJC7
    nsv5013709copy number variation1nstd200human GRCh38 chr17: 41,980,038-41,981,366 , GRCh37.p13 chr17|NW_003571052.1: 266,680-268,008 , GRCh37.p13 chr17: 40,132,056-40,133,384 DNAJC7
    nsv4858841copy number variation1nstd200human GRCh37 chr17: 40,133,359-40,133,612 , GRCh38.p12 chr17: 41,981,341-41,981,594 DNAJC7
    nsv4858840copy number variation1nstd200human GRCh37 chr17: 40,129,596-40,130,621 , GRCh38.p12 chr17: 41,977,578-41,978,603 DNAJC7, CNP
    nsv4680071copy number variation1nstd189human GRCh37.p13 chr17: 39,432,725-40,293,644 , GRCh38.p12 chr17: 41,276,473-42,141,626 ACLY, CNP, 50 more genes
    nsv4513936mobile element insertion1nstd166human GRCh37.p13 chr17: 40,164,031-40,164,031 , GRCh38.p12 chr17: 42,012,013-42,012,013 DNAJC7
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